Literature DB >> 10792464

Functional interaction of general transcription initiation factor TFIIE with general chromatin factor SPT16/CDC68.

S W Kang1, T Kuzuhara, M Horikoshi.   

Abstract

BACKGROUND: Transcriptional initiation of class II genes is one of the major targets for the regulation of gene expression and is carried out by RNA polymerase II and many auxiliary factors, which include general transcription initiation factors (GTFs). TFIIE, one of the GTFs, functions at the later stage of transcription initiation. As recent studies indicated the possibility that TFIIE may have a role in chromatin transcriptional regulation, we isolated TFIIE-interacting factors which have chromatin-related functions.
RESULTS: Using the yeast two-hybrid screening system, we isolated the C-terminal part of the human homologue of Saccharomyces cerevisiae (y) Spt16p/Cdc68p, a general chromatin factor. The C-terminal part of human SPT16/CDC68 directly interacts with TFIIE, and ySpt16p/Cdc68p also interacts with yTFIIE (Tfa1p/Tfa2p), thus indicating the existence of an evolutionarily conserved interaction between TFIIE and SPT16/CDC68. Functional interaction of yTFIIE and ySpt16p/Cdc68p was examined using a conditional yTFIIE-alpha mutant strain. Over-expression of ySpt16p/Cdc68p suppressed the phenotype of cold sensitivity of the yTFIIE-alpha-cs mutant strain, and in vitro binding assays revealed that yTFIIE-alpha-cs mutant protein showed diminished binding affinity to ySpt16p/Cdc68p.
CONCLUSIONS: These observations indicate that general transcription initiation factor TFIIE functionally interacts with general chromatin factor SPT16/CDC68, a finding which provides new insight into the involvement of TFIIE in chromatin transcription. This may well lead to a breakthrough in relationships between the transcription initiation process and structural changes in chromatin.

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Year:  2000        PMID: 10792464     DOI: 10.1046/j.1365-2443.2000.00323.x

Source DB:  PubMed          Journal:  Genes Cells        ISSN: 1356-9597            Impact factor:   1.891


  6 in total

1.  The histone chaperone facilitates chromatin transcription (FACT) protein maintains normal replication fork rates.

Authors:  Takuya Abe; Kazuto Sugimura; Yoshifumi Hosono; Yasunari Takami; Motomu Akita; Akari Yoshimura; Shusuke Tada; Tatsuo Nakayama; Hiromu Murofushi; Katsuzumi Okumura; Shunichi Takeda; Masami Horikoshi; Masayuki Seki; Takemi Enomoto
Journal:  J Biol Chem       Date:  2011-07-07       Impact factor: 5.157

2.  Spt16-Pob3 and the HMG protein Nhp6 combine to form the nucleosome-binding factor SPN.

Authors:  T Formosa; P Eriksson; J Wittmeyer; J Ginn; Y Yu; D J Stillman
Journal:  EMBO J       Date:  2001-07-02       Impact factor: 11.598

3.  The Modifier of Transcription 1 (Mot1) ATPase and Spt16 Histone Chaperone Co-regulate Transcription through Preinitiation Complex Assembly and Nucleosome Organization.

Authors:  Jason D True; Joseph J Muldoon; Melissa N Carver; Kunal Poorey; Savera J Shetty; Stefan Bekiranov; David T Auble
Journal:  J Biol Chem       Date:  2016-05-16       Impact factor: 5.157

4.  The FACT complex travels with elongating RNA polymerase II and is important for the fidelity of transcriptional initiation in vivo.

Authors:  Paul B Mason; Kevin Struhl
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

5.  FACT, the Bur kinase pathway, and the histone co-repressor HirC have overlapping nucleosome-related roles in yeast transcription elongation.

Authors:  Jennifer R Stevens; Allyson F O'Donnell; Troy E Perry; Jeremy J R Benjamin; Christine A Barnes; Gerald C Johnston; Richard A Singer
Journal:  PLoS One       Date:  2011-10-12       Impact factor: 3.240

6.  Histone Chaperones Spt6 and FACT: Similarities and Differences in Modes of Action at Transcribed Genes.

Authors:  Andrea A Duina
Journal:  Genet Res Int       Date:  2011-10-26
  6 in total

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